Take advantage of our $1795.00 price by registering early!
* After Friday, September 27, 2019, costs are $1995.00.
Clinical Research Coordinator (CRC) has a vital role in the conduct of a
clinical trial and is a key liaison between the investigator, subject, IRB, and
sponsor. The online 10-Week Clinical Research Coordinator (CRC) On-Boarding
Program will provide a comprehensive introduction to clinical research and the
job functions of the CRC for both drug/biologic and device trials. This program
will provide core skills and encourage critical thinking to those individuals
looking to support, facilitate, and coordinate the daily activities of clinical
Case studies and industry
best practices will be presented to underscore how the learning objectives
apply directly to the responsibilities of the CRC.
The resources required to
take this on-line course are already at your fingertips - an Internet
connection and a phone. After registering, you will receive an email
confirmation that provides you with the Web Seminar link and audio connection
Prior to the start of the
course, participants will receive comprehensive course materials. Come to class
prepared to interact – you will be able to ask questions, provide feedback and
participate in discussions and group work. Upon course completion, participants
will be provided training certificates. In order to receive accreditation CEUs,
participants are required to pass both a mid-term and final exam. Upon
completion of the exams, CEU certificates will be provided.
- Understand the roles and responsibilities of the
Clinical Research Coordinator
- Prepare for what a pharmaceutical or
device sponsor is looking for in a research site during a pre-study
evaluation or site selection visit
- Understand the requirements for
source documentation, case report forms, study tool development, and
standard operating procedures (SOPs)
- Define informed consent requirements
and learn the process of conducting informed consent
- Define safety reporting: Definitions
and reporting requirements
- Discuss regulatory compliance and
quality assurance as it relates to audits and inspections
- Module 1: Introduction to Clinical Research, Investigational Product Development: Drug and Device, Regulatory Oversight, and Good Clinical Practice Guidelines
- Module 2: The Clinical Research
Team: Roles and Responsibilities
- Module 3: The Principal
Investigator and Site Selection
- Module 4: Clinical Study Protocol
Breakdown and Feasibility Evaluation
- Module 5: Source Documentation,
Case-Report Forms, Study Tool Development, and Standard Operating
- Module 6: Informed Consent
Requirements and Process
- Module 7: Study Initiation,
Start-up, and Ongoing Management Activities and Sponsor Expectations
- Module 8: Safety Reporting:
Definitions and Reporting Requirements
- Module 9: Accountability for the
Test Article and the Trial Termination Visit
- Module 10: Regulatory Compliance
and Quality Assurance: Audits and Inspection
- Aspiring CRCs (This course is also appropriate
for CRCs with less than six months of experience)
- College Students and New Graduates
in a Scientific Field
- Nurses interested in developing
skills in clinical research
NOTE: This course is for
individual registrants only and does not allow for group training.
What participants say about Barnett's 10-Week courses
“Great course! Instruction is expertly led and engaging. I
will recommend Barnett to any colleague and will seek out topics for my own
future training and professional development needs.”
"The course has been so incredibly helpful thus far...I
look forward to Thursday evenings!"
“This class exceeded my expectations of an online learning
experience. The instructor was knowledgeable, came equipped with great examples
to keep the class interesting and is a strong presenter. Thank you!”
The course will be led by one of the following
Janet Ellen Holwell, C.C.R.C., C.C.R.A., T.I.A.C.R., F.A.C.R.P.
Angie Maurer, R.N., B.S.N., M.B.A.
Click here for complete trainer
10 weeks for 2 hours each week.
$1,795 by Early Bird Deadline
$1,995 after Early Bird Deadline
This course is for individual
registrants only and does not allow for group training.
All participants are eligible for
“Certificates of Attendance,” and accreditation, provided that accreditation
requirements are met.
Barnett International is
accredited by the Accreditation Council for Pharmacy Education as a provider of
continuing pharmacy education. Participants will receive 30 hours (3.0
CEUs) of continuing education credit for full participation, including the
completion of a mid-term exam, final exam, and program
evaluation. Barnett International will issue a receipt of completion
for earned CEUs within three weeks of program completion. ACPE#:
0778-0000-17-015-L01-P. Released: 3/17.
this course at your company! For more information, contact Naila Ganatra at +1